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63136-19-6

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63136-19-6 Usage

General Description

4-Chloro-8-ethylquinoline is a chemical compound that belongs to the class of quinoline derivatives. It is a yellowish liquid with a molecular formula C11H10N. 4-CHLORO-8-ETHYLQUINOLINE is primarily used as an intermediate in the production of pharmaceuticals and agrochemicals. It has also shown potential as a building block in the synthesis of various organic compounds. 4-Chloro-8-ethylquinoline is known to have antimicrobial and antifungal properties, making it useful in the development of drugs and treatments for various diseases. Additionally, it can be utilized in the manufacturing of dyes and fluorescent materials due to its unique electronic and structural properties.

Check Digit Verification of cas no

The CAS Registry Mumber 63136-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63136-19:
(7*6)+(6*3)+(5*1)+(4*3)+(3*6)+(2*1)+(1*9)=106
106 % 10 = 6
So 63136-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClN/c1-2-8-4-3-5-9-10(12)6-7-13-11(8)9/h3-7H,2H2,1H3

63136-19-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-8-ethylquinoline

1.2 Other means of identification

Product number -
Other names 4-chloro-8-ethyl-quinoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63136-19-6 SDS

63136-19-6Upstream product

63136-19-6Downstream Products

63136-19-6Relevant articles and documents

Catalytic Enantioselective Methylene C(sp3)?H Amidation of 8-Alkylquinolines Using a Cp*RhIII/Chiral Carboxylic Acid System

Fukagawa, Seiya,Kojima, Masahiro,Yoshino, Tatsuhiko,Matsunaga, Shigeki

supporting information, p. 18154 - 18158 (2019/11/22)

Catalytic enantioselective directed methylene C(sp3)?H amidation reactions of 8-alkylquinolines using a Cp*RhIII/chiral carboxylic acid (CCA) hybrid catalytic system are described. A binaphthyl-based chiral carboxylic acid efficiently differentiates between the enantiotopic methylene C?H bonds, which leads to the formation of C?N bonds with good enantioselectivity.

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